Hydrogen Bromide → Benzaldehyde, 2,3-dihydroxy-4-nitro-
反応式
C([O:4][C:5]1[C:12]([O:13]C)=[C:11]([N+:15]([O-:17])=[O:16])[CH:10]=[CH:9][C:6]=1[CH:7]=[O:8])(=O)C.Br>C(O)(=O)C>[OH:4][C:5]1[C:12]([OH:13])=[C:11]([N+:15]([O-:17])=[O:16])[CH:10]=[CH:9][C:6]=1[CH:7]=[O:8]参加物
4
反応条件
- 温度
- 150 °C
実験手順
43 (2.5 g, 10.5 mmol) was added to a solution of acetic acid (62.5 mL) and hydrobromic acid 48% (70 mL) and the reaction mixture was heated at 150° C. for 4 h. The reaction mixture was then cooled to rt and evaporated to dryness. The residue was diluted in hot CH2Cl2 (40 mL) and filtered. The filtrate was evaporated to dryness to give 44 (1.74 g, 91%) which was used as such in the next step:
後処理
- temperatureThe reaction mixture was then cooled to rt
- customevaporated to dryness
- additionThe residue was diluted in hot CH2Cl2 (40 mL)
- filtrationfiltered
- customThe filtrate was evaporated to dryness
出典と根拠
- ORDレコード
- ord-ff0c615cad7d4dd096e5f930998f45a0
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08198302B2
反応ノート
読み込み中…